Variant #0000003336 (NC_000018.9:-, DSG2(NM_001943.3):c.462C>A)
Chromosome |
18 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Type |
In particular, a C!A transversion
in exon 5 resulting in the substitution of an aspartic acid
wi |
DNA change (genomic) (Relative to hg19 / GRCh37) |
- |
Reference |
GenBank |
DB-ID |
DSG2_00023 |
Frequency |
- |
Variant remarks |
462C>A |
ClassClinical |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Qi Ming |
Database submission license |
No license selected |
Created by |
Qi Ming |

Variant on transcripts
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